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Allele-specific variation at APOE increases nonalcoholic fatty liver disease and obesity but decreases risk of Alzheimer’s disease and myocardial infarction
- Source :
- Human molecular genetics, vol 30, iss 15, Hum Mol Genet
- Publication Year :
- 2021
- Publisher :
- Oxford University Press (OUP), 2021.
-
Abstract
- Nonalcoholic fatty liver disease (NAFLD) is a leading cause of chronic liver disease and is highly correlated with metabolic disease. NAFLD results from environmental exposures acting on a susceptible polygenic background. This study performed the largest multiethnic investigation of exonic variation associated with NAFLD and correlated metabolic traits and diseases. An exome array meta-analysis was carried out among eight multiethnic population-based cohorts (n = 16 492) with computed tomography (CT) measured hepatic steatosis. A fixed effects meta-analysis identified five exome-wide significant loci (P
- Subjects :
- Liver Cirrhosis
0301 basic medicine
Apolipoprotein E
Aging
Cirrhosis
Myocardial Infarction
Disease
Neurodegenerative
Alzheimer's Disease
Chronic liver disease
Medical and Health Sciences
Gastroenterology
Oral and gastrointestinal
Hepatitis
Liver disease
0302 clinical medicine
Gene Frequency
Risk Factors
Non-alcoholic Fatty Liver Disease
Databases, Genetic
Nonalcoholic fatty liver disease
2.1 Biological and endogenous factors
Exome
Aetiology
Association Studies Article
Genetics (clinical)
Genetics & Heredity
Liver Disease
Fatty liver
Alanine Transaminase
Single Nucleotide
General Medicine
Biological Sciences
Prognosis
Phenotype
Liver
Biotechnology
medicine.medical_specialty
Chronic Liver Disease and Cirrhosis
Biology
Polymorphism, Single Nucleotide
Databases
03 medical and health sciences
Apolipoproteins E
Genetic
Alzheimer Disease
Internal medicine
Acquired Cognitive Impairment
Genetics
medicine
Humans
Obesity
Polymorphism
Molecular Biology
Triglycerides
Alleles
Prevention
Human Genome
Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD)
medicine.disease
Brain Disorders
030104 developmental biology
Dementia
Steatosis
Digestive Diseases
030217 neurology & neurosurgery
Genome-Wide Association Study
Subjects
Details
- ISSN :
- 14602083 and 09646906
- Volume :
- 30
- Database :
- OpenAIRE
- Journal :
- Human Molecular Genetics
- Accession number :
- edsair.doi.dedup.....0a1410659c19fddb97f8c0e22ad4dda1
- Full Text :
- https://doi.org/10.1093/hmg/ddab096